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New insights for IL-6 targeted therapy as an adjuvant treatment for non-small-cell lung cancer

机译:IL-6靶向治疗作为非小细胞肺癌辅助治疗的新见解

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摘要

IL-6 has been identified as a powerful cyto-kine that is responsible for carcinogenesis, neo-angiogenesis, malignant transformation and distant metastasis [1]. Increased levels of IL-6 have been associated with increased risk of cancer development for the general population, but also for nonsmoking women with asthma/atopy [2]. IL-6 has been identified as a biomarker significantly associated with overall survival, advanced stage cancer [3,4] and with early cancer recurrence after curative lung cancer surgery [5]. IL-6 has been identified as a late biomarker for lung cancer risk development (<2 years); however, IL-8 has been identified as an early biomarker for cancer (>2 years) [2]. The levels of IL-6 have been directly associated with chemotherapy treatment response in lung cancer patients [3]. In the case of targeted therapy in lung cancer patients with tyrosine kinase inhibitors (TKIs) it was observed that although the treatment was effective, the levels of IL-6 increased and increased production of a-actin and collagen [6].
机译:IL-6被认为是一种强大的细胞因子,可导致癌变,新血管生成,恶性转化和远处转移[1]。 IL-6水平升高与普通人群癌症发病风险增加有关,但对于患有哮喘/动脉粥样硬化的非吸烟女性也是如此[2]。 IL-6已被鉴定为与整体生存,晚期癌症[3,4]和治愈性肺癌手术后的早期癌症复发显着相关的生物标志物[5]。 IL-6已被确定为肺癌风险发展的晚期生物标志物(<2年);然而,IL-8已被确定为癌症的早期生物标志物(> 2年)[2]。 IL-6的水平与肺癌患者的化疗反应直接相关[3]。在针对具有酪氨酸激酶抑制剂(TKIs)的肺癌患者进行靶向治疗的情况下,已观察到尽管治疗有效,但IL-6的水平增加并增加了α-肌动蛋白和胶原蛋白的产生[6]。

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